Background: Consumption of moderate amounts of alcohol has been reported to
exert a cardioprotective effect in individuals. The exact mechanism by whi
ch this occurs has npt been fully explored. Circulating levels of the dotti
ng protein fibrinogen have been unequivocally established as an independent
risk factor for vascular diseases. This study examined the effects of mode
rate levels of ethanol on the expression of fibrinogen in an animal model a
nd in hepatoma cells.
Methods: Out-bred Sprague-Dawley rats were fed 5% ethanol (v/v) in their wa
ter for 4 weeks, and circulating levels of fibrinogen were measured weekly
via quantitative immunoassay. H4IIE rat hepatoma cells, which constitutivel
y produce fibrinogen, were exposed to 10 and 20 mM ethanol, and fibrinogen
production was determined. The effects of ethanol on fibrinogen messenger r
ibonucleic acids were determined by northern gel analyses.
Results: Our findings demonstrate that daily consumption of moderate amount
s of ethanol decreases circulating levels of fibrinogen 18% to 20%. The dec
rease is reversible and is not gender specific. The exposure of hepatoma ce
lls to ethanol also diminishes fibrinogen production by 20% by decreasing t
he transcription of fibrinogen genes. Alcohol concentration of 10 to 20 mM
did not affect hepatoma cell viability or doubling time.
Conclusions: The findings indicate that one likely positive benefit of mode
rate ethanol consumption is to diminish the production of fibrinogen, which
reduces the potential risk exerted by this protein. The site of action of
ethanol is, at least in part, exerted at the level of gene transcription.